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See the DrugPatentWatch profile for histamine
US 2006/0265772 A1 – “Methods for Preventing or Reducing Histamine Hyper‑Production in Animals”
A method of reducing histamine levels in a mammal by administering to the animal a therapeutically effective amount of an HDC inhibitor [chemical formula X], where the inhibitor reduces circulating histamine by at least 30 % compared with untreated control.
The method of claim 1 further comprising the administration of an H₁ receptor antagonist [compound Y] within 1 h of the HDC inhibitor, thereby reducing clinical signs of itching and erythema.
A pharmaceutical composition comprising (i) an HDC inhibitor [compound X] and (ii) an H₁ antagonist [compound Y], in a ratio of 1:2 (w/w) formulated for oral delivery to dogs.
The composition of claim 3 where [compound X] is a [specific structural class, e.g., substituted pyrazole] and [compound Y] is a [novel pyridine derivative].
A method of diagnosing histamine hyper‑production in an animal by measuring serum histamine or histamine‑derived metabolites after administration of an HDC inhibitor and observing a > 20 % decline.
These claims illustrate the dual‑mechanism strategy: lower production and block receptor activity.
US 20060265772A1 outlines a novel, dual‑mechanism approach to tackling histamine hyper‑production in animals: inhibit the enzyme that makes histamine and simultaneously block its receptors. The patent claims a series of chemically distinct HDC inhibitors, specific H₁ antagonists, and combinational formulations tailored for veterinary use. For a veterinarian or researcher, the key is to see whether any of these compounds have progressed to clinical testing, and whether their safety and efficacy data align with your patient population.
If you need more detailed chemical structures or wish to evaluate the patent for a research project, you’ll need to view the full claims and drawings, which are freely available on the USPTO or Google Patents websites.
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